MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2017-06-14 for DR COMFORT 2440-W-10.5 manufactured by Dr Comfort, A Djo, Llc Company.
[77558114]
Not returned.
Patient Sequence No: 1, Text Type: N, H10
[77558115]
Complaint received that alleges "caused her big toenail on her right foot to turn black. She had to have the toenail surgically removed. " questionnaire not received from customer or clinician. Device not returned to manufacturer for evaluation.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3008579854-2017-00002 |
MDR Report Key | 6641013 |
Report Source | DISTRIBUTOR |
Date Received | 2017-06-14 |
Date of Report | 2017-06-14 |
Date of Event | 2017-06-02 |
Date Added to Maude | 2017-06-14 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | WILLIAM FISHER |
Manufacturer Street | 1430 DECISION STREET |
Manufacturer City | VISTA CA 920819663 |
Manufacturer Country | US |
Manufacturer Postal | 920819663 |
Manufacturer G1 | DR COMFORT, A DJO, LLC COMPANY |
Manufacturer Street | 10300 ENTERPRISE DRIVE |
Manufacturer City | MEQUON 53092 |
Manufacturer Country | US |
Manufacturer Postal Code | 53092 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DR COMFORT |
Generic Name | SPIRIT X WHITE VELCRO 10 1/2 W |
Product Code | KNP |
Date Received | 2017-06-14 |
Model Number | 2440-W-10.5 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DR COMFORT, A DJO, LLC COMPANY |
Manufacturer Address | 10300 ENTERPRISE DRIVE MEQUON 53092 US 53092 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-06-14 |